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Complement-Related Regulates Autophagy in Neighboring Cells

  • Lin Lin
  • , Frederico S.L.M. Rodrigues
  • , Christina Kary
  • , Alicia Contet
  • , Mary Logan
  • , Richard H.G. Baxter
  • , Will Wood
  • , Eric H. Baehrecke
  • University of Massachusetts Medical School
  • Carnegie Institution of Washington
  • University of Bristol
  • Nature Cell Biology
  • Yale University
  • Oregon Health and Science University

Research output: Contribution to journalArticlepeer-review

53 Scopus citations

Abstract

Autophagy degrades cytoplasmic components and is important for development and human health. Although autophagy is known to be influenced by systemic intercellular signals, the proteins that control autophagy are largely thought to function within individual cells. Here, we report that Drosophila macroglobulin complement-related (Mcr), a complement ortholog, plays an essential role during developmental cell death and inflammation by influencing autophagy in neighboring cells. This function of Mcr involves the immune receptor Draper, suggesting a relationship between autophagy and the control of inflammation. Interestingly, Mcr function in epithelial cells is required for macrophage autophagy and migration to epithelial wounds, a Draper-dependent process. This study reveals, unexpectedly, that complement-related from one cell regulates autophagy in neighboring cells via an ancient immune signaling program.

Original languageEnglish
Pages (from-to)158-171.e8
JournalCell
Volume170
Issue number1
DOIs
StatePublished - Jun 29 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Animals
  • Autophagy
  • Complement System Proteins/immunology
  • Cytokines
  • Drosophila Proteins
  • Drosophila melanogaster/cytology
  • Inflammation/immunology
  • Larva/growth & development
  • Macrophages/immunology
  • Salivary Glands/cytology
  • Serpins

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